Canonical Allele Identifier: CA3902870

Gene: BCKDHB

Linked Data

• dbSNP Id: rs370684959
• ExAC: 6:81053556 T / C
• gnomAD v2: 6-81053556-T-C
• gnomAD v3: 6-80343839-T-C
• gnomAD v4: 6-80343839-T-C
• MyVariant Identifiers: chr6:g.81053556T>C (hg19) ; chr6:g.80343839T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343839T>C , CM000668.2:g.80343839T>C	GRCh38
NC_000006.11:g.81053556T>C , CM000668.1:g.81053556T>C	GRCh37
NC_000006.10:g.81110275T>C	NCBI36
NG_009775.1:g.242213T>C
NG_009775.2:g.242213T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.*35T>C MANE Select	ENSP00000318351.5:n.*35T>C
ENST00000320393.8:c.*35T>C	ENSP00000318351.5:n.*35T>C
ENST00000356489.9:c.*8+27T>C	ENSP00000348880.5:n.*8+27T>C
ENST00000491328.1:n.242+27T>C
NM_000056.3:c.*8+27T>C	NP_000047.1:n.*8+27T>C
NM_183050.2:c.*35T>C	NP_898871.1:n.*35T>C
NM_000056.4:c.*8+27T>C	NP_000047.1:n.*8+27T>C
NM_001318975.1:c.*35T>C	NP_001305904.1:n.*35T>C
NM_183050.3:c.*35T>C	NP_898871.1:n.*35T>C
NR_134945.1:n.1392T>C
XM_011536024.3:c.*220T>C	XP_011534326.1:n.*220T>C
XR_001743546.2:n.1068+70618T>C
XR_001743547.2:n.1068+70618T>C
XR_001743548.2:n.1068+70618T>C
XR_001743549.2:n.1068+70618T>C
XR_002956292.1:n.1068+70618T>C
NM_183050.4:c.*35T>C MANE Select	NP_898871.1:n.*35T>C
NR_134945.2:n.1331T>C
NM_000056.5:c.*8+27T>C	NP_000047.1:n.*8+27T>C